Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3747517
rs3747517
13 0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 0.710 1.000 3 2012 2016
dbSNP: rs1990760
rs1990760
33 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 0.710 1.000 2 2012 2015
dbSNP: rs35667974
rs35667974
9 0.776 0.280 2 162268127 missense variant T/C snv 1.1E-02 1.2E-02 0.710 1.000 2 2010 2016
dbSNP: rs72871627
rs72871627
5 0.827 0.120 2 162280432 intron variant A/G snv 7.1E-03 0.700 1.000 1 2016 2016
dbSNP: rs10930046
rs10930046
3 0.882 0.200 2 162281473 missense variant T/C snv 9.7E-02 0.16 0.010 1.000 1 2010 2010